Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_provenance.
- NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_assertion description "[None of the NAT2 (classified as slow vs. fast acetylator), ESR1 or ESR2 polymorphisms were significantly associated with an altered risk of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_provenance.
- NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_assertion evidence source_evidence_literature NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_provenance.
- NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_assertion SIO_000772 20304699 NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_provenance.
- NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_assertion wasDerivedFrom befree-20150227 NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_provenance.
- NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_assertion wasGeneratedBy ECO_0000203 NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP217776.RAiqsk2dN4FlYQ3q-UrXO_1IoQcUlT7907tw1v26uAXF8130_provenance.